(Q36821490)

English

Clinical and prognostic evaluation of familial hypertrophic cardiomyopathy in two South African families with different cardiac beta myosin heavy chain gene mutations

scientific article published on July 1995

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Statements

scholarly article

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

Clinical and prognostic evaluation of familial hypertrophic cardiomyopathy in two South African families with different cardiac beta myosin heavy chain gene mutations (English)

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

0 references

hypertrophic cardiomyopathy

1 reference

based on heuristic

inferred from title

familial hypertrophic cardiomyopathy

1 reference

based on heuristic

inferred from title

author name string

Posen BM

1

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

Moolman JC

2

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

Corfield VA

3

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

Brink PA

4

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

publication date

1 July 1995

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

British Heart Journal

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

74

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

1

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

40-46

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

Mapping of a novel gene for familial hypertrophic cardiomyopathy to chromosome 11

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=483944

29 September 2017

A familial hypertrophic cardiomyopathy locus maps to chromosome 15q2.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=483944

29 September 2017

Genotype-phenotype correlations in hypertrophic cardiomyopathy. Insights provided by comparisons of kindreds with distinct and identical beta-myosin heavy chain gene mutations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=483944

29 September 2017

Familial hypertrophic cardiomyopathy. Microsatellite haplotyping and identification of a hot spot for mutations in the beta-myosin heavy chain gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=483944

29 September 2017

Molecular genetics of familial hypertrophic cardiomyopathy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=483944

29 September 2017

Arrhythmia in hypertrophic cardiomyopathy. I: Influence on prognosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=483944

29 September 2017

Hypertrophic cardiomyopathy. Interrelations of clinical manifestations, pathophysiology, and therapy (2).

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=483944

29 September 2017

Hypertrophic cardiomyopathy. Interrelations of clinical manifestations, pathophysiology, and therapy (1).

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=483944

29 September 2017

Hypertrophic cardiomyopathy: current views on etiology, pathophysiology, and management

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=483944

29 September 2017

Detection of human papilloma virus in paraffin-embedded tissue using the polymerase chain reaction

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=483944

29 September 2017

The complete sequence of the human beta-myosin heavy chain gene and a comparative analysis of its product

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=483944

29 September 2017

A molecular basis for familial hypertrophic cardiomyopathy: a beta cardiac myosin heavy chain gene missense mutation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=483944

29 September 2017

Differences in clinical expression of hypertrophic cardiomyopathy associated with two distinct mutations in the beta-myosin heavy chain gene. A 908Leu----Val mutation and a 403Arg----Gln mutation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=483944

29 September 2017

“Malignant” hypertrophic cardiomyopathy: Identification of a subgroup of families with unusually frequent premature death

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=483944

29 September 2017

A disease locus for familial hypertrophic cardiomyopathy maps to chromosome 1q3.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=483944

27 June 2018

Localization of gene for familial hypertrophic cardiomyopathy to chromosome 14q1 in a diverse US population

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=483944

27 June 2018

Characteristics and prognostic implications of myosin missense mutations in familial hypertrophic cardiomyopathy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=483944

27 June 2018

Identification of a new missense mutation at Arg403, a CpG mutation hotspot, in exon 13 of the beta-myosin heavy chain gene in hypertrophic cardiomyopathy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=483944

5 September 2018

Prognostic significance of 24 hour ambulatory electrocardiographic monitoring in patients with hypertrophic cardiomyopathy: a prospective study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=483944

5 September 2018

A point-score system for the ECG diagnosis of left ventricular hypertrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/7662452

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Electrocardiographic findings in patients with obstructive and nonobstructive hypertrophic cardiomyopathy

1 reference

https://pubmed.ncbi.nlm.nih.gov/7662452

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Sudden death in young athletes

1 reference

https://pubmed.ncbi.nlm.nih.gov/7662452

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Patterns and significance of distribution of left ventricular hypertrophy in hypertrophic cardiomyopathy. A wide angle, two dimensional echocardiographic study of 125 patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/7662452

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Relation of electrocardiographic abnormalities to evolving left ventricular hypertrophy in hypertrophic cardiomyopathy during childhood

1 reference

https://pubmed.ncbi.nlm.nih.gov/7662452

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Sudden death in hypertrophic cardiomyopathy. Assessment of patients at high risk

1 reference

https://pubmed.ncbi.nlm.nih.gov/7662452

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mapping a gene for familial hypertrophic cardiomyopathy to chromosome 14q1

1 reference

https://pubmed.ncbi.nlm.nih.gov/7662452

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Evidence of genetic heterogeneity in five kindreds with familial hypertrophic cardiomyopathy

1 reference

https://pubmed.ncbi.nlm.nih.gov/7662452

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Polymerase chain reaction-based detection of MN blood group-specific sequences in the human genome

1 reference

https://pubmed.ncbi.nlm.nih.gov/7662452

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1136/HRT.74.1.40

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

ResearchGate publication ID

0 references

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